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HRID 1111498作成日:2026年10月26日

Tetrahydrofuran → 4-(4-Formylcyclohexyl)benzonitrile

https://huagongshe.com/reaction/1111498

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物p-[4-(Methoxymethylene)cyclohexyl]benzonitrileHCID 19739357—
溶媒WaterHCID 962—
生成物4-(4-Formylcyclohexyl)benzonitrileHCID 11769829100%

反応手順

A mixture of 4.2 g of p-[4-(methoxymethylene)cyclohexyl]benzonitrile and 100 ml of tetrahydrofuran/2N hydrochloric acid (vol. 4:1) was heated to reflux for 30 minutes in a round flask. The mixture was subsequently poured into 100 ml of water and extracted three times with 100 ml of diethyl ether each time The organic phases were washed once with 100 ml of water, dried over magnesium sulphate and concentrated There were obtained 3.9 g (100%) of 4-(p-cyanophenyl)cyclohexanecarboxaldehyde as a colourless oil which was used in the next step without further purificarion: trans/cis ratio about 3:1, Rf-value (ethyl acetate/petroleum ether, vol. 3:7) 0.41. By recrystallization from hexane there could be obtained pure trans-4 (p-cyanophenyl)cyclohexanecarboxaldehyde; m.p. 57.1° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04980486
出典データセットuspto-grants-1990_12
ORD IDord-b1a963f121af4e11a3e10c9c616588d7
出典メモuspto-grants-1990_12